Particle engineering for pulmonary drug delivery

被引:523
作者
Chow, Albert H. L. [1 ]
Tong, Henry H. Y.
Chattopadhyay, Pratibhash
Shekunov, Boris Y.
机构
[1] Chinese Univ Hong Kong, Sch Pharm, Shatin, Hong Kong, Peoples R China
[2] Ferro Pfanstiehl Labs, Pharmaceut Technol, Independence, OH 44131 USA
关键词
aerosols; crystalline and amorphous solids; inhalers; micro- and nanoparticles; micronization; particle size; respiratory drug delivery; spray drying; spray freeze drying; supercritical fluids;
D O I
10.1007/s11095-006-9174-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
With the rapidly growing popularity and sophistication of inhalation therapy, there is an increasing demand for tailor-made inhalable drug particles capable of affording the most efficient delivery to the lungs and the most optimal therapeutic outcomes. To cope with this formulation demand, a wide variety of novel particle technologies have emerged over the past decade. The present review is intended to provide a critical account of the current goals and technologies of particle engineering for the development of pulmonary drug delivery systems. These technologies cover traditional micronization and powder blending, controlled solvent crystallization, spray drying, spray freeze drying, particle formation from liquid dispersion systems, supercritical fluid processing and particle coating. The merits and limitations of these technologies are discussed with reference to their applications to specific drug and/or excipient materials. The regulatory requirements applicable to particulate inhalation products are also reviewed briefly.
引用
收藏
页码:411 / 437
页数:27
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